The N1 domain of the peroxisomal AAA-ATPase Pex6 is required for Pex15 binding and proper assembly with Pex1

被引:0
|
作者
Ali, Bashir [1 ]
Judy, Ryan [1 ]
Chowdhury, Saikat [1 ]
Jacobsen, Nicole [1 ]
Castanzo, Dominic [1 ]
Richardson, Chris [1 ]
Martin, Andreas [1 ]
Lander, Gabriel [1 ]
Gardner, Brooke [1 ]
机构
[1] Univ Calif Santa Barbara, Santa Barbara, CA 93106 USA
关键词
ATPases associated with diverse cellular activities (AAA); Peroxisome; protein assembly; protein-protein interaction; allosteric regulation;
D O I
10.1016/j.jbc.2024.106674
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1466
引用
收藏
页码:S521 / S521
页数:1
相关论文
共 50 条
  • [31] Recruiting Mechanism of the AAA Peroxins, Pex1p and Pex6p, to Pex26p on the Peroxisomal Membrane
    Nashiro, Chika
    Kashiwagi, Astuko
    Matsuzaki, Takashi
    Tamura, Shigehiko
    Fujiki, Yukio
    TRAFFIC, 2011, 12 (06) : 774 - 788
  • [32] Crystallographic characterization of the N-terminal domain of PEX1
    Shiozawa, K
    Maita, N
    Tomii, K
    Seto, A
    Goda, N
    Akiyama, Y
    Shimizu, T
    Shirakawa, M
    Hiroaki, H
    ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 : 2098 - 2099
  • [33] The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes
    Matsumoto, N
    Tamura, S
    Fujiki, Y
    NATURE CELL BIOLOGY, 2003, 5 (05) : 454 - 460
  • [34] Structures of the double-ring AAA ATPase Pex1-Pex6 involved in peroxisome biogenesis
    Tan, Dongyan
    Blok, Neil B.
    Rapoport, Tom A.
    Walz, Thomas
    FEBS JOURNAL, 2016, 283 (06) : 986 - 992
  • [35] The AAA peroxins Pex1p and Pex6p function as dislocases for the ubiquitinated peroxisomal import receptor Pex5p
    Platta, Harald W.
    Debelyy, Mykhaylo O.
    El Magraoui, Fouzi
    Erdmann, Ralf
    BIOCHEMICAL SOCIETY TRANSACTIONS, 2008, 36 : 99 - 104
  • [36] The pathogenic peroxin Pex26p recruits the Pex1p–Pex6p AAA ATPase complexes to peroxisomes
    Naomi Matsumoto
    Shigehiko Tamura
    Yukio Fujiki
    Nature Cell Biology, 2003, 5 : 454 - 460
  • [37] Peroxisomal membrane fusion requires two AAA family ATPases, Pex1p and Pex6p
    Titorenko, VI
    Rachubinski, RA
    JOURNAL OF CELL BIOLOGY, 2000, 150 (04): : 881 - 886
  • [38] Defects in PEX1, a peroxisome-associated ATPase that interacts with PEX6, are the most common cause of Zellweger syndrome, neonatal adrenoleukodystrophy and infantile Refsum disease.
    Germain-Lee, E
    Morrell, JC
    Geisbrecht, B
    Collins, C
    Ameritunga, R
    Moser, HW
    Valle, D
    Gould, SJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A54 - A54
  • [39] Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p
    Tamura, Shigehiko
    Yasutake, Shinobu
    Matsumoto, Naomi
    Fujiki, Yukio
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (38) : 27693 - 27704
  • [40] The AAA-type ATPases Pex1p and Pex6p and their role in peroxisomal matrix protein import in Saccharomyces cerevisiae
    Grimm, Immanuel
    Saffian, Delia
    Platta, Harald W.
    Erdmann, Ralf
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2012, 1823 (01): : 150 - 158